Pairing probiotics and prebiotics, methods for growth and use, separately and in combination

ABSTRACT

A method for growing probiotic organisms wherein the growth media includes prebiotics especially selected and prepared to be paired with the probiotic organisms being grown. The prebiotic formula is optimized to grow the desired probiotic organisms, as well as important byproducts of the growth process. Specialized freeze-drying buffers may also be paired with certain probiotic organisms for the freeze-drying process.

RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Patent Application Ser. No. 62/655,935, filed on Apr. 11, 2018, which is hereby incorporated by reference in its entirety.

BACKGROUND 1. The Field of the Invention

This invention relates to methods for producing probiotics, and more particularly to the pairing of particular probiotics and prebiotics to optimize growth and usefulness of the probiotics.

2. Background

Numerous products contain probiotics for a variety of purposes. These purposes may include regulating digestion, improving and maintaining health in general, or improving specific physiological systems, as well as other purposes. The probiotic Lactobacillus acidophilus is an example of the use of probiotics as a nutritional supplement, or as a component in foods such as yogurts.

Generally, probiotics may be grown or cultured using a broth and/or an agar spread plate. There are various formulations for such a broth and various media used for such agar spread plates. These formulations are relatively standardized for both broths and agar spread plates.

Methods for growing and culturing common probiotics, like Lactobacillus acidophilus, are generally established. For example, an original strain of the desired probiotic may be obtained and used an inoculation material. The inoculation material may be grown in a fermenter (i.e., a liquid broth) and/or on a surface (i.e., an agar plate). This growth generally happens under pre-defined and monitored conditions. The grown probiotic may then be harvested. After being harvested, the probiotic may be blended with other probiotics. The single probiotic or blend of probiotics may be preserved in some manner for transportation and/or storage.

While there are various, useful probiotics that are found in nature, not all probiotics are available for commercial use. What is needed is an improved method or methods for culturing and harvesting more types of probiotics. Moreover, to get the full benefit of certain probiotics, those probiotics should be cultured or grown with the most appropriate prebiotics, or prebiotics specifically matched to optimize the growth of the desired probiotics. What is needed is an improved method or methods for producing or culturing various, useful probiotics to fully realize the potential and benefits of those probiotics.

BRIEF SUMMARY OF THE INVENTION

In accordance with the foregoing, certain embodiments of a probiotic product and/or method for production in accordance with the invention may provide probiotics that can be used for a variety of purposes, including without limitation, nutritional supplements, topical applications, and related uses and products.

There are a number of probiotic organisms that may be considered useful and helpful to promote or maintain health in humans and animals. Such probiotics may include Bacteroides thetaiotaomicron, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Faecalibacterium prausnitzii, Akkermansia muciniphila, Eubacterium rectale, Collinsella aerofaciens, Desulfovibrio piger, Clostridium symbiosum, Mycobacterium vaccae, Eubacterium limosum, Butyricicoccus pullicaecorum, Roseomonas mucosa, Lactobacillus farciminis, Staphylococcus epidermis, Staphylococcus xylosus, Pediococcus acidilactici, Roseburia hominis, and Anaerostipes caccae. These probiotics, and methods for growing them, are primarily described herein, but the methods and formulations described herein may be applicable to other probiotic organisms.

A method for growing probiotic organisms, or growing unique probiotic fermentations, may comprise a number steps. The method may include selecting a probiotic organism to grow. The method may include selecting a growth broth for growing the probiotic organism, wherein the growth broth includes a prebiotic formulation that is optimized for the selected probiotic organism. The method may include inoculating the growth broth with the probiotic organism. The method may include growing the probiotic organism in the growth broth and harvesting the probiotic organism from the growth broth. The method may include selecting an agar spread plate for growing the probiotic organism, wherein the agar spread plate media includes a prebiotic formula that is optimized for growing the probiotic organism. The method may include inoculating the agar spread plate with the probiotic organism harvested from the growth broth. The method may include growing the probiotic organism on the agar spread plate and harvesting the probiotic organism from the agar spread plate.

A method may further include freeze-drying the harvested probiotic organism with a lyophilization reagent. The lyophilization reagent may be comprised of one or more of the following: glucosamine, glutamine, sucrose, mannitol, trehalose, glycerol, inositol, raffinose, inulin, powdered skim milk, activated charcoal, soluble starch, collagen powder, chondroitin sulfate, glucosamine sulfate, guar, acacia, silica, and fructooligosaccharide P95.

A method as described herein may be used for growing any of the probiotic organisms included, as well as other probiotic organisms. A method may include the use of a specific formulation of prebiotics that are optimized for, or preferentially paired with, specific probiotic organisms. This pairing of certain prebiotics with certain probiotics helps promote better and faster growth of the desired probiotic. The use of certain, important prebiotics can promote the growth of a probiotic organism and specific byproducts of importance. Thus, a prebiotic, or prebiotic formulation, may be selected to be paired with a probiotic organism both for growing the probiotic organism and a desired byproduct, or group of byproducts, that may be helpful or important for a given purpose.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing features of the present invention will become more fully apparent from the following description and appended claims, taken in conjunction with the accompanying drawings and experimental data. Understanding that these drawings and date depict only typical embodiments of the invention and are, therefore, not to be considered limiting of its scope, the invention will be described with additional specificity and detail through use of the accompanying drawings and data in which:

FIG. 1 illustrates a table providing results of measuring the amount of certain short chain fatty acids produced from certain probiotic organisms, where the values for short chain fatty acids are in milligrams per milliliter measured from culture supernatant; and

FIG. 2 is a schematic diagram of an embodiment of a method for growing probiotic organisms.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

It will be readily understood that the components of the present invention, as generally described herein, could be arranged and designed in a wide variety of different configurations or formulations. Thus, the following more detailed description of the embodiments of the system, product and method of the present invention, is not intended to limit the scope of the invention, as claimed, but is merely representative of various embodiments of the invention.

In one embodiment, a method for growing or culturing numerous probiotic organisms may include the following steps: selecting a probiotic organism, or a group of probiotic organisms, to grow; selecting a growth broth, which may include a prebiotic formulation specially designed to help grow the probiotic organism selected; growing the probiotic organism in the growth broth; harvesting the probiotic organism from the growth broth; selecting a growth plate, which may include a prebiotic formulation specially designed to help grow the probiotic organism selected; growing the probiotic organism on the growth plate; and harvesting the probiotic organism from the growth plate.

A probiotic organism, or a group of organisms, grown in this manner can be freeze-dried after harvesting to prepare the organism for transfer and/or storage.

The various steps in the process for growing a probiotic organism may include variations at every level. For example, and not by way of limitation, a growth broth may or may not include a prebiotic formula specially selected for the probiotic organism being grown. A prebiotic formula may be specifically designed for one or more probiotic organisms, thereby allowing for numerous and varied formulations for prebiotic formulas. Also, the conditions for growing certain probiotic organisms can vary.

Generally, a probiotic organism grown in accordance with the disclosed method will be one or more of the following: Bacteroides thetaiotaomicron, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Faecalibacterium prausnitzii, Akkermansia muciniphila, Eubacterium rectale, Collinsella aerofaciens, Desulfovibrio piger, Clostridium symbiosum, Mycobacterium vaccae, Eubacterium limosum, Butyricicoccus pullicaecorum, Roseomonas mucosa, Lactobacillus farciminis, Staphylococcus epidermis, Staphylococcus xylosus, Pediococcus acidilactici, Roseburia hominis, and Anaerostipes caccae.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 26 grams of tryptic soy broth, approximately 4 grams of inulin, and approximately 0.4 grams of cysteine in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Eubacterium limosum, and Clostridium symbiosum.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 26 grams of tryptic soy broth, approximately 4 grams of inulin, approximately 0.4 grams of cysteine, and approximately 3.6 milliliters of 50% glycerol in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Bacteroides thetaiotaomicron.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 26 grams of tryptic soy broth, approximately 4 grams of inulin, approximately 2.5 grams of Middlebrook 7H9 broth, and approximately 7.2 milliliters of 50% glycerol in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Mycobacterium vaccae. This probiotic organism may be grown aerobically.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 50 grams of MRS broth, approximately 0.1 grams of glutathione, approximately 0.4 grams of cysteine, and approximately 0.2 grams of uric acid in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Collinsella aerofaciens.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 50 grams of MRS broth in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Pediococcus acidilactici and Lactobacillus farciminis. These probiotic organisms may be grown aerobically or anaerobically.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 33 grams of brain heart infusion, approximately 0.1 grams of glutathione, approximately 0.4 grams of cysteine, approximately 8 grams of inulin, approximately 4.5 grams of yeast extract, and approximately 1.8 grams of sodium acetate in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Faecalibacterium prausnitzii.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 7 grams of nutrient broth, approximately 4.5 grams of tryptone, approximately 9 grams of yeast extract, approximately 8 grams of inulin, approximately 4.5 grams of dextrose, approximately 1.5 grams of dipotassium phosphate (K₂HPO₄), approximately 4.5 milliliters of 20% tween 80, approximately 0.4 grams of cysteine, and approximately 27 milliliters of a salt solution in approximately 900 milliliters of water. The salt solution may be comprised of approximately 0.2 grams of calcium chloride (CaCl₂), approximately 0.24 grams of magnesium sulfate (MgSO₄), approximately 1.0 grams of monopotassium phosphate (KH₂PO₄), approximately 10 grams of sodium bicarbonate (NaHCO₃), and approximately 2.0 grams of sodium chloride (NaCl) in approximately one liter of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Eubacterium rectale, Anaerostipes caccae, and Butyricicoccus pullicaecorum.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 33 grams of brain heart infusion, approximately 1.0 grams of mucin, and approximately 0.4 grams of cysteine in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Akkermansia muciniphila.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 27 grams of tryptic soy broth, approximately 4 grams of yeast extract, approximately 0.8 grams of sodium lactate, approximately 0.4 grams of magnesium sulfate, approximately 0.3 grams of ferric ammonium sulfate-6H₂O, approximately 0.4 grams of cysteine, and approximately 0.1 grams of glutathione in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Desulfovibrio piger.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 50 grams of MRS broth, approximately 0.4 grams of cysteine, approximately 0.1 grams of glutathione, and approximately 27 milliliters of a salt solution in approximately 900 milliliters of water. The salt solution may be comprised of approximately 0.2 grams of calcium chloride (CaCl₂), approximately 0.24 grams of magnesium sulfate (MgSO₄), approximately 1.0 grams of monopotassium phosphate (KH₂PO₄), approximately 10 grams of sodium bicarbonate (NaHCO₃), and approximately 2.0 grams of sodium chloride (NaCl) in approximately one liter of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Roseburia hominis.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 7 grams of nutrient broth in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Roseomonas mucosa.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 27 grams of tryptic soy broth in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Staphylococcus epidermidis. This probiotic organism may be grown aerobically or anaerobically.

In one embodiment, a growth broth, or liquid growth medium, may be comprised of approximately 27 grams of tryptic soy broth and approximately 7.2 milliliters of 50% glycerol in approximately 900 milliliters of water. Such a growth broth may be kept and/or used in a sealed one liter bottle. Such a growth broth may be used to grow a probiotic organism, for example and not by way of limitation, Staphylococcus xylosus. This probiotic organism may be grown aerobically or anaerobically.

In one embodiment, an agar spread plate media, or agar spread plate, may be comprised of approximately 40 g/L tryptic soy agar, approximately 50 ml/L defibrinated sheep blood, approximately 0.5 g/L cysteine, and approximately 0.1 g/L glutathione. Such an agar spread plate may be used to grow a probiotic organism, for example and not by way of limitation, Bacteroides thetaiotaomicron, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Eubacterium limosum, Clostridium symbiosum, Collinsella aerofaciens, Faecalibacterium prausnitzii, Eubacterium rectale, Roseburia hominis, Anaerostipes caccae, Butyricicoccus pullicaecorum, Roseomonas mucosa, Staphylococcus epidermidis, and Staphylococcus xylosus.

In one embodiment, an agar spread plate media, or agar spread plate, may be comprised of approximately 12 g/L agar and a growth broth (approximately 3 g/L) comprised of approximately 26 grams of tryptic soy broth, approximately 4 grams of inulin, approximately 2.5 grams of Middlebrook 7H9 broth, and approximately 7.2 milliliters of 50% glycerol in approximately 900 milliliters of water. Such an agar spread plate may be used to grow a probiotic organism, for example and not by way of limitation, Mycobacterium vaccae. This probiotic organism may be grown aerobically.

In one embodiment, an agar spread plate media, or agar spread plate, may be comprised of approximately 70 g/L of MRS agar. Such an agar spread plate may be used to grow a probiotic organism, for example and not by way of limitation, Pediococcus acidilactici and Lactobacillus farciminis. These probiotic organisms may be grown aerobically or anaerobically.

In one embodiment, an agar spread plate media, or agar spread plate, may be comprised of approximately 12 g/L agar and a growth broth (approximately 3 g/L) comprised of approximately 33 grams of brain heart infusion, approximately 1.0 grams of mucin, and approximately 0.4 grams of cysteine in approximately 900 milliliters of water. A pour plate may use 8 g/L agar. Such an agar spread plate may be used to grow a probiotic organism, for example and not by way of limitation, Akkermansia muciniphila.

In one embodiment, an agar spread plate media, or agar spread plate, may be comprised of approximately 10 g/L agar and a growth broth (approximately 3 g/L) comprised of approximately 27 grams of tryptic soy broth, approximately 4 grams of yeast extract, approximately 0.8 grams of sodium lactate, approximately 0.4 grams of magnesium sulfate, approximately 0.3 grams of ferric ammonium sulfate-6H₂O, approximately 0.4 grams of cysteine, and approximately 0.1 grams of glutathione in approximately 900 milliliters of water. A pour plate may use 10 g/L agar. Such an agar spread plate may be used to grow a probiotic organism, for example and not by way of limitation, Desulfovibrio piger.

In one embodiment, a freeze-drying buffer, or lyophilization buffer, may be used to freeze-dry probiotic organisms that are grown and harvested. Freeze-drying reagents, or lyophilization reagents, may include the following compounds alone or in combination: glucosamine, sucrose, mannitol, trehalose, glycerol, inositol, raffinose, inulin, powdered skim milk, activated charcoal, soluble starch, collagen powder, chondroitin sulfate, glucosamine sulfate, glutamine, guar, acacia, silica, and fructooligosaccharide P95. A freeze-drying buffer, or lyophilization buffer, may be comprised of appropriate amounts of one or more of the freeze-drying reagents in deionized water, which is then adjusted to a pH of 7.0 with potassium hydroxide.

In one embodiment, a freeze-drying buffer may be made at least one day prior to the freeze-drying process. A freeze-drying buffer may be stored overnight in an anaerobic chamber to allow dissolved oxygen to escape the solution. The volume of a freeze-drying buffer used may be equal to the volume of a cell pellet or probiotic organisms obtained after centrifugation.

In one embodiment, a freeze-drying buffer or media may be made with anti-oxidant and growth factors, for example and not by way of limitation, cysteine, ascorbic acid, glutathione, uric acid, riboflavin, glutamic acid, sodium sulfite, and quinones.

In one embodiment, a freeze-drying buffer, or lyophilization buffer, may be comprised of 10% mannitol, 12.5% sucrose, 2.5% trehalose, 1.0% glycerol, 10% skim milk, 0.02% cysteine, 0.01% ascorbic acid, 0.005% glutathione, 0.005% uric acid, and 2.0% charcoal in deionized water and adjusted to pH 7 with potassium hydroxide. The percentages provided may be considered approximate percentages. This embodiment of a freeze-drying buffer will hereinafter be referred to as “Freeze-drying Buffer A.” Freeze-drying Buffer A may be used with various probiotic organisms, for example and not by way of limitation, Mycobacterium vaccae, Pediococcus acidilactici, Roseomonas mucosa, Lactobacillus farciminis, Staphylococcus epidermidis, and Staphylococcus xylosus.

In one embodiment, a freeze-drying buffer, or lyophilization buffer, may be comprised of 10% mannitol, 12.5% sucrose, 2.5% trehalose, 1.0% glycerol, 10% skim milk, 0.2% cysteine, 0.1% ascorbic acid, 0.05% glutathione, 0.05% uric acid, and 2.0% charcoal in deionized water and adjusted to pH 7 with potassium hydroxide. The percentages provided may be considered approximate percentages. This embodiment of a freeze-drying buffer will hereinafter be referred to as “Freeze-drying Buffer B.” Freeze-drying Buffer B may be used with various probiotic organisms, for example and not by way of limitation, Bacteroides thetaiotaomicron, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Eubacterium limosum, Collinsella aerofaciens, Akkermansia muciniphila, and Roseburia hominis.

In one embodiment, a freeze-drying buffer, or lyophilization buffer, may be comprised of 10% mannitol, 10% inulin, 5% short chain FOS, 10% soluble starch, 2.5% trehalose, 1.0% glycerol, 2.0% cysteine, 0.5% ascorbic acid, 0.5% glutathione, 0.1% uric acid, and 6.0% charcoal in deionized water and adjusted to pH 7 with potassium hydroxide. The percentages provided may be considered approximate percentages. This embodiment of a freeze-drying buffer will hereinafter be referred to as “Freeze-drying Buffer C.” Freeze-drying Buffer C may be used with various probiotic organisms, for example and not by way of limitation, Clostridium symbiosum, Faecalibacterium praunsnitzii, Eubacterium rectale, Anaerostipes caccae, and Butyricicoccus pullicaecorum.

In one embodiment, a freeze-drying buffer, or lyophilization buffer, may be comprised of 10% mannitol, 12.5% sucrose, 2.5% trehalose, 10% collagen powder, 1.0% chondroitin sulfate, 1.0% glycerol, 2.0% cysteine, 0.5% ascorbic acid, 0.5% glutathione, 0.1% uric acid, and 6.0% charcoal in deionized water and adjusted to pH 7 with potassium hydroxide. The percentages provided may be considered approximate percentages. This embodiment of a freeze-drying buffer will hereinafter be referred to as “Freeze-drying Buffer D.” Freeze-drying Buffer D may be used with various probiotic organisms, for example and not by way of limitation, Desulfovibrio piger.

In one embodiment, a dilution buffer, or anti-oxidant resuspension solution, may be utilized for plating lyophilized bacteria and/or obtaining plate counts and estimating cfu/gram (colony-forming unit per gram of sample). In one embodiment, a dilution buffer, or anti-oxidant resuspension solution, may be comprised of 0.2% cysteine, 0.1% ascorbic acid, 0.05% glutathione, 0.05% uric acid, and 0.0425% monopotassium phosphate (KH₂PO₄) monopotassium phosphate (KH₂PO₄) in deionized water and adjusted to pH 7 with potassium hydroxide solution.

Culture conditions for various probiotic organisms have been determined experimentally.

In one embodiment, various probiotic organisms, for example and not by way of limitation, Bacteroides thetaiotaomicron, Bacteroides fragilis, Bacteroides ovatus, Bacteroides uniformis, Eubacterium limosum, Collinsella aerofaciens, Akkermansia muciniphila, and Desulfovibrio piger require 48-96 hours of incubation at 37° C. to achieve the desired growth. The addition of anti-oxidants during media preparation may be required, but no special anaerobic conditions are required for growth in liquid media, or growth broth. The liquid media bottles should be capped to prevent contamination and to limit airflow to the growing probiotic cultures. Disturbance of the liquid media, such as swirling, should be avoided to limit oxygen rich air being mixed with the liquid media.

Centrifugation and freeze-drying processes can be performed in an aerobic environment if done quickly, for example, by mixing the centrifuged pellet with a freeze-dry buffer immediately after pouring off the supernatant and then placing the suspension at −20° C. It may take approximately one hour to fully freeze the suspension. Then the suspension can be placed in the lyophilizer.

Spread plating or pour plating techniques can be used for these probiotic organisms, provided that the dilution buffer, or antioxidant resuspension solution, is used. Plates should be put in an anaerobic chamber or airtight box containing anaerobic gas producing packets. Growth of colonies on plates typically requires 24-72 hours at 37° C.

In one embodiment, various probiotic organisms, for example and not by way of limitation, Clostridium symbiosum, Faecalibacterium prausnitzii, Eubacterium rectale, Roseburia hominis, Anaerostipes caccae, and Butyricicoccus pullicaecorum require 24-48 hours of incubation at 37° C. to achieve desired growth. These probiotic organisms grow poorly unless incubated in an oxygen-free environment. Oxygen rich air must be evacuated from liquid media bottles before placing them in an anaerobic chamber.

For centrifugation, liquid cultures must be poured into airtight centrifuge bottles and sealed in an anaerobic chamber. The centrifuge bottles can then be removed from the chamber to undergo centrifugation. They must be placed back in the anaerobic chamber before opening to pour off the supernatant. The cell pellets are then suspended in freeze-dry buffer that has been sitting in the anaerobic chamber overnight, or for approximately twelve hours, to help pull off oxygen dissolved in the buffer. The cell suspension is then sealed in an airtight container and placed at −20° C. until lyophilized in aerobic conditions.

All plating techniques must be performed in the anaerobic chamber. Growth of colonies on plates typically requires 24-48 hours at 37° C.

In one embodiment, various probiotic organisms, for example and not by way of limitation, Mycobacterium vaccae, Pediococcus acidilactici, Roseomonas mucosa, Lactobacillus farciminis, Staphylococcus epidermidis, and Staphylococcus xylosus require 24-48 hours of incubation at 37° C. to achieve desired growth, except that M. vaccae may require 5-8 days. These probiotic organisms may be cultured aerobically. Aeration of liquid media, or growth broth, using a stir plate and a stir bar improves growth of M. vaccae, R. mucosa, and S. xylosus.

Centrifugation, any freeze-drying process, and plate growth techniques may all occur in an aerobic environment. Colonies on plates are typically observed in 24-48 hours at 37° C., except that M. vaccae may take 3-5 days.

Prebiotic formulations may be used to supplement, support, and optimize probiotic growth, which process may be referred to as synbiotics. In order to facilitate growth of a given probiotic organism, the correct or matching prebiotic is crucial. Since probiotic organisms vary in genus and species, specific prebiotic preparations or formulations may be required. Some prebiotics colonize the lumen and others the mucus layers. Many prebiotics are butyrate-producing Firmicutes members.

Prebiotics often enhance mucosal butyrate, which has been shown to possibly stimulate the release of mucosal butyrate producers towards the lumen. A process connected with that may affect the intestinal inflammation and consumption of prebiotic compounds.

Some probiotic organisms require other special conditions like co-culturing with another commensal organism. For example and not by way of limitation, Bacteroides fragilis produces GABA (Gamma-Aminobutyric Acid), a metabolite required by a second organism. Therefore, the two organisms may be considered co-dependent.

Various techniques may be utilized to introduce a prebiotic, or a prebiotic formulation, to a method for growing a certain probiotic organism, or multiple probiotic organisms. In one embodiment, a growth media may be exogenously supplemented with the needed metabolite. In another embodiment, the supernatant of one organism may be used to supplement the growth media used for growing another organism of interest. For example and not by way of limitation, growth of Faecalibacterium prausnitzii may require special supplementation of one or more specific vitamin K metabolites.

Table 1 below describes a prebiotic formulation that may be used with probiotic organisms including Faecalibacterium prausnitzii, Mycobacterium vaccae, and Lactobacillus farciminis.

TABLE 1 Prebiotic mg/dose Galacto-oligosaccharide 3000.0 Isomalt-oligosaccharide 3000.0 IgY-immunoglobulin 100.0 Deoxynojirimycin polysaccharide (DPM) 500.0 Lactoferrin 50.0 Guggulipids 500.0 Sorghum 2000.0 Pectin 1000.0 Fructooligosaccharide (FOS) 1000.0 Blueberry powder 1000.0 Black currant 1000.0 Lions mane mushroom 500.0 Cordyceps militarus 500.0 Karaya gum 500.0 Ellagitanin (from promegrante) 500.0 Dehydroellagitanin (from Geranium thunbergii) 500.0 Geraniin and furosin (from Phyllanthus muellerianus) 500.0 Gallic ellagic (from raspberry extract) 500.0 Total 16650.0

The amounts in Table 1 may be considered approximations. The prebiotic formulation represented in Table 1 may be hereinafter referred to as “Prebiotic Formula Alpha.”

Table 2 below describes a prebiotic formulation that may be used with probiotic organisms including Eubacterium limosum, Bacteroides thetaiotaomicron, Lactobacillus vaginalis, and Bacteroides uniformis.

TABLE 2 Prebiotic mg/dose Glycomacropeptide 1000.0 Xylo-oligosaccharide 1000.0 Glucomannan 1000.0 Inulin; sprouted greens 1000.0 Galactomannan 1000.0 Blueberry powder 1000.0 Thymus 1000.0 Mulberry leaves 1000.0 Myo-inositol 1000.0 Modified citrus pectin 1000.0 Tapioca 500.0 Glucosaminoglycan 1000.0 Guar sun-fiber 500.0 Oat oligosaccharide 500.0 Clitoria ternatea (blue pea flower) 500.0 Cranberry extract 500.0 Bearberry (Arctostaphylos uva-ursi) 500.0 Total 14000.0

The amounts in Table 2 may be considered approximations. The prebiotic formulation represented in Table 2 may be hereinafter referred to as “Prebiotic Formula Beta.”

Table 3 below describes a prebiotic formulation that may be used with probiotic organisms including Bacteroides ovatus, Anaerostipes caccae, Staphylococcus xylosus, Staphylococcus epidermidis, and Roseomonas mucosa.

TABLE 3 Prebiotic mg/dose 2′ fructosyllactose 2000.0 Isomato-oligosaccharide 1000.0 Fructooligosaccharide Yacon root/Beneo/innulin 1000.0 Galactooligosaccharide 1000.0 Rutin 1000.0 Oat oligosaccharide 1000.0 Sialylated bovine milk oligosaccharides (S-BMO) 1000.0 IgY immunoglobulin 1000.0 Beta glucan 1000.0 Maca 1000.0 Lactooligosaccharide 1000.0 Medium Chain Triglycerides 500.0 Phosphatidyl choline 500.0 Rose hips/organic green banana 500.0 Citrus bioflavonoids 500.0 Colostrum 500.0 Total 14500.0

The amounts in Table 3 may be considered approximations. The prebiotic formulation represented in Table 3 may be hereinafter referred to as “Prebiotic Formula Gamma.”

Table 4 below describes a prebiotic formula that may be used with probiotic organisms including Collinsella aerofaciens, Bacteroides ovatus, Bacteroides uniformis, Clostridium symbiosum, Bacteroides fragilis, and Roseburia hominis.

TABLE 4 Prebiotic mg/dose Galactooligosaccharide 2000.0 Mannan-oligosaccharide 1000.0 Resveratrol 1000.0 Hesperetin 1000.0 Arabinoxylan oligosaccharides 1000.0 Dragon fruit 1000.0 Beechwood extract xylan 1000.0 Arabinogalactan (Larix laricina) 1000.0 DAO antihistamine 1000.0 Xanthan gum 1000.0 Resistant starch 1000.0 Baobab fruit 500.0 Kongorobi berry 1000.0 Resveratrol/Pterostilbene 500.0 Curcumin 500.0 Indian Tinospora (Tinospora cordifolia)(stem and root) 500.0 Poria mushroom 500.0 Total 15500.0

The amounts in Table 4 may be considered approximations. The prebiotic formulation represented in Table 4 may be hereinafter referred to as “Prebiotic Formula Delta.”

The various prebiotic formulations may be utilized with a liquid media or growth broth. The prebiotic formulation selected and paired with a given probiotic organism may constitute approximately 1%-15% of the growth broth. Similarly, the various prebiotic formulations may be utilized with an agar spread plate. The prebiotic formulation selected and paired with a given probiotic organism may constitute approximately 1%-15% of the agar spread plate media.

Prebiotic ingredients used in prebiotic formulations can many different types of compounds. For example and not by way of limitation, complex plant oligosaccharides may include the following: Galacto-oligosaccharide; Isomalt-oligosaccharide; Mannan-oligosaccharide; Apple pectin oligosaccharide; Xylo-oligosaccharide; and Fructo-oligosaccharide-inulin. These complex plant oligosaccharides have been shown increase caecal mucin levels by approximately six-fold and correspond with even higher butyrate levels and higher abundances of the same mucosal butyrate producers.

Other complex plant oligosaccharides include Oat-oligosaccharides and Arabinoxylan-oligosaccharides (AXOS), which have been shown to be a promising class of prebiotics that stimulate the growth of Bifidobacterium longum, an acetate producer to stimulate Eubacterium rectale, an acetate-converting butyrate producer.

Another complex plant oligosaccharide is Deoxynojirimycin polysaccharide (DPM), which has been shown to increase the Bacteroides to Firmicutes ratios, significantly inhibiting the growth of Prevotella, and increasing the relative abundance of Bacteroides, Lactobacillus, Bifidobacterium, and Akkermansia in mice.

Animal based oligosaccharides may include the following: N-acetyl glucosamine-amino glycan Lactulose-saccharide; IgY-immunoglobulin; and Sialylated bovine milk oligosaccharides (S-BMO).

Other complex prebiotic compounds may include the following: Cyclodextrin-saccharide; Mulberry-cyanadins; Maca-oligosaccharides; polyphenols; Rutin-flavonoid (E. limosum specifically metabolized flavonoids); mushroom-polysaccharides; aminoglycans; Shilajit (organic compounds); Resveratrol; and Pterostilbene.

The criteria for pairing or partnering certain probiotic organisms with specific prebiotics is driven by the metabolites that are produced by the probiotic organisms. For example and not by way of limitation, the metabolites produced by probiotic organisms that may be evaluated to pair or partner those probiotic organisms with specific prebiotics may include the following: small chain fatty acids, such as butyric acid, acetic acid, propionic acid, hexanoic acid, and the like; organic acids, such as lactic acid, malic acid, citric acid, and the like; bacteriocins, which are natural antimicrobials produced by probiotic organisms. The research and analysis required to properly partner probiotic organisms and prebiotic compounds can take years to complete.

FIG. 1 provides an example of the research conducted and evaluated to properly partner probiotic organisms and prebiotic compounds based on the production of short chain fatty acids produced in selected strains of probiotic organisms. The values for short chain fatty acids in FIG. 1 are in milligrams per milliliter measured from culture supernatant.

In one embodiment, a phage may be used as a terrain biotic. For example and not by way of limitation, terrain biotics may include Streptococcus mutans, Actinomyces naeslundi, Cutibacterium acnes, Porphyromonas gingivalis, Treponema denticola, Fusobactium nucleatum, Aggregatibacter actinomycetemcomitans, and Tannerella forsythia.

Referring to FIG. 2, one embodiment of a method 10 for producing probiotic organisms may include the steps of selecting a probiotic organism to grow 15, selecting a prebiotic formula 20 to pair with the probiotic organism selected, selecting a growth broth 25, inoculating the growth broth 30, growing the probiotic organism 35, harvesting the probiotic organism from the growth broth 40, selecting a growth plate 45, inoculating the growth plate 50, growing the probiotic organism on the growth plate 55, harvesting the probiotic organism from the growth plate 60, and freeze-drying the probiotic organism 65.

The step of selecting a probiotic organism to grow 15 can be based on numerous factors. The uses, properties, and metabolites of a given probiotic organism may be considered. Generally, the process of beginning to grow a probiotic organism will start with a pure strain of the organism, but it is possible to grow multiple probiotic organisms together. However, more care should be taken to select organisms that can be grown using the same growth media, as well as the same prebiotic formulations, to optimize growth of all probiotic organisms selected.

The step of selecting a prebiotic formula, or formulation, 20 to grow the selected probiotic organism should be based primarily on the probiotic organism selected. The intention is to match or partner the prebiotics with the probiotic organism as best as can be done to promote optimal growth of the probiotic organism. For example and not by way of limitation, if Mycobacterium vaccae is the probiotic organism selected to be grown, Prebiotic Formula Alpha would be an optimal choice for prebiotics to pair with the probiotic organism during the growth process.

The step of selecting a growth broth 25, or selecting a liquid media for growth 25, may include a number of factors. A growth broth can be selected based on the particular probiotic organism to be grown, and there are certain growth broths that can be used to grow specific probiotic organisms. Also, a growth broth may include at least some of a prebiotic formulation to promote the growth process. A growth broth may be augmented to include a prebiotic formula where the prebiotic formula is approximately 1%-15% of the growth broth media. For example and not by way of limitation, if Bacteroides fragilis is the probiotic organism to be grown, the growth broth used (and previously described) may be augmented to be approximately 10% Prebiotic Formula Delta.

The step of inoculating the growth broth 30 is generally performed by introducing the selected probiotic organism into the selected and prepared growth broth by any appropriate means.

The step of growing the probiotic organism in the growth broth 35 is accomplished by any appropriate means. For example and not by way of limitation, if Bacteroides fragilis is the probiotic organism to be grown, the growth broth may be kept in a sealed bottle and allowed to incubate for 48-96 hours at 37° C. For example and not by way of limitation, if Mycobacterium vaccae is the probiotic organism to be grown, the growth should take place anaerobically.

The step of harvesting the probiotic organism from the growth broth 40 is generally accomplished by any appropriate means that are consistent with the requirements for the probiotic organism. For example and not by way of limitation, if Mycobacterium vaccae is the probiotic organism to be grown, this harvesting process should take place anaerobically.

The step of selecting a growth plate 45, or selecting an agar spread plate for growing the selected probiotic organism 45, may include consideration of multiple factors. The type of media used for the growth plate should be compatible with the probiotic organism to be grown. Also, the media of the growth plate may include a prebiotic formulation to promote growth of the probiotic organism. For example and not by way of limitation, if Bacteroides thetaiotaomicron is the probiotic organism to be grown, the growth plate used, or agar spread plate used (and previously described), may be augmented to include approximately 5% Prebiotic Formula Beta.

The step of inoculating the growth plate 50, or inoculating and/or preparing the agar spread plate 50, is generally performed by introducing the probiotic organism harvested from the growth broth 40 onto the surface of the selected and prepared growth plate by any appropriate means. For example and not by way of limitation, if Roseburia hominis is the probiotic organism to be grown, the inoculating and/or preparing the growth plate should take place anaerobically.

The step of growing the probiotic organism on the growth plate 55, or growing the probiotic organism on the agar spread plate 55, is accomplished by any appropriate means. For example and not by way of limitation, if Bacteroides fragilis is the probiotic organism to be grown, the growth plate may be allowed to incubate for 24-72 hours at 37° C. For example and not by way of limitation, if Mycobacterium vaccae is the probiotic organism to be grown, the growth should take place anaerobically.

The step of harvesting the probiotic organism from the growth plate 60 is generally accomplished by any appropriate means that are consistent with the requirements for the probiotic organism. For example and not by way of limitation, if Mycobacterium vaccae is the probiotic organism to be grown, this harvesting process should take place anaerobically.

The step of freeze-drying the probiotic organism 65 may include consideration of a variety of factors. There may be times when the freeze-drying step is not required or desired. The probiotic organism may require preparation for storage and/or delivery. Also, a specially prepared buffer for the freeze-dry process, or freeze-drying buffer, may be utilized for lyophilization of a specific probiotic organism. For example and not by way of limitation, if Clostridium symbiosum is the probiotic organism that has been grown, then Freeze-drying Buffer C may be used to more appropriately freeze-dry that probiotic organism.

The subject invention may be more easily comprehended by reference to the specific embodiments recited herein, which are representative of the invention. However, it must be understood that the specific embodiments are provided only for the purpose of illustration, and that the invention may be practiced in a manner separate from what is specifically illustrated without departing from its scope and spirit. 

What is claimed and desired to be secured by United States Letters Patent is:
 1. A method for growing probiotic organisms comprising: selecting a probiotic organism to grow, which is selected from the group consisting of Faecalibacterium prausnitzii, Mycobacterium vaccae, and Lactobacillus farciminis; selecting a growth broth for growing the probiotic organism, wherein the growth broth comprises 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 and/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the growth broth with the probiotic organism; growing the probiotic organism in the growth broth; harvesting the probiotic organism from the growth broth; selecting an agar spread plate for growing the probiotic organism, wherein an agar spread plate media comprises 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 and/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the agar spread plate with the probiotic organism harvested from the growth broth; growing the probiotic organism on the agar spread plate; and harvesting the probiotic organism from the agar spread plate.
 2. The method of claim 1, further comprising: freeze-drying the probiotic organism.
 3. The method of claim 1, further comprising: freeze-drying the probiotic organisms harvested from the agar spread plate by use of a Freeze-drying Buffer A when the probiotic organism is at least one probiotic organism selected from the group consisting of Mycobacterium vaccae and Lactobacillus farciminis, wherein Freeze-drying Buffer A comprises 10% mannitol, 12.5% sucrose, 2.5% trehalose, 1.0% glycerol, 10% skim milk, 0.02% cysteine, 0.01% ascorbic acid, 0.005% glutathione, 0.005% uric acid, and 2.0% charcoal present in deionized water and adjusted to pH 7 with potassium hydroxide.
 4. The method of claim 1, further comprising: freeze-drying the probiotic organism harvested from the agar spread plate by use of a lyophilization reagent, wherein the lyophilization reagent includes at least two compounds selected from the group consisting of glucosamine, glutamine, sucrose, mannitol, trehalose, glycerol, inositol, raffinose, inulin, powdered skim milk, activated charcoal, soluble starch, collagen powder, chondroitin sulfate, glucosamine sulfate, guar, acacia, silica, and fructooligosaccharide P95.
 5. The method of claim 3, further comprising: using the probiotic organism in a nutritional supplement product.
 6. The method of claim 4, further comprising: using the probiotic organism in a topical application product.
 7. A method for growing probiotic organisms comprising: selecting at least two probiotic organisms to grow, which are selected from the group consisting of Faecalibacterium prausnitzii, Mycobacterium vaccae, and Lactobacillus farciminis; selecting a growth broth for growing the probiotic organisms, wherein the growth broth consists essentially of 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 and/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the growth broth with the probiotic organisms; growing the probiotic organisms in the growth broth; harvesting the probiotic organisms from the growth broth; selecting an agar spread plate for growing the probiotic organisms, wherein an agar spread plate media consists essentially of 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 and/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the agar spread plate with the probiotic organisms harvested from the growth broth; growing the probiotic organisms on the agar spread plate; and harvesting the probiotic organisms from the agar spread plate.
 8. The method of claim 7, further comprising: freeze-drying the probiotic organisms.
 9. The method of claim 7, further comprising: freeze-drying the probiotic organisms harvested from the agar spread plate by use of a Freeze-drying Buffer A when the probiotic organisms are Mycobacterium vaccae and Lactobacillus farciminis, wherein Freeze-drying Buffer A comprises 10% mannitol, 12.5% sucrose, 2.5% trehalose, 1.0% glycerol, 10% skim milk, 0.02% cysteine, 0.01% ascorbic acid, 0.005% glutathione, 0.005% uric acid, and 2.0% charcoal present in deionized water and adjusted to pH 7 with potassium hydroxide.
 10. The method of claim 7, further comprising: freeze-drying the probiotic organisms harvested from the agar spread plate by use of a lyophilization reagent, wherein the lyophilization reagent includes at least two compounds selected from the group consisting of glucosamine, glutamine, sucrose, mannitol, trehalose, glycerol, inositol, raffinose, inulin, powdered skim milk, activated charcoal, soluble starch, collagen powder, chondroitin sulfate, glucosamine sulfate, guar, acacia, silica, and fructooligosaccharide P95.
 11. The method of claim 9, further comprising: using the probiotic organisms in a nutritional supplement product.
 12. The method of claim 10, further comprising: using the probiotic organisms in a topical application product.
 13. A method for growing probiotic organisms comprising: selecting a probiotic organism to grow, which is selected from the group consisting of Faecalibacterium prausnitzii, Mycobacterium vaccae, and Lactobacillus farciminis; selecting a growth broth for growing the probiotic organism, wherein the growth broth consists of 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 md/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the growth broth with the probiotic organism; growing the probiotic organism in the growth broth; harvesting the probiotic organism from the growth broth; selecting an agar spread plate for growing the probiotic organism, wherein an agar spread plate media consists of 3000.0 mg/dose Galacto-oligosaccharide, 3000.0 mg/dose Isomalt-oligosaccharide, 100.0 mg/dose IgY-immunoglobulin, 500.0 mg/dose Deoxynojirimycin polysaccharide (DPM), 50.0 mg/dose Lactoferrin, 500.0 mg/dose Guggulipids, 2000.0 mg/dose Sorghum, 1000.0 mg/dose Pectin, 1000.0 mg/dose Fructooligosaccharide (FOS), 1000.0 mg/dose Blueberry powder, 1000.0 mg/dose Black currant, 500.0 mg/dose Lions mane mushroom, 500.0 md/dose Cordyceps militarus, 500.0 mg/dose Karaya gum, 500.0 mg/dose ellagitanin from Pomegranate, 500.0 mg/dose dehydroellagitanin from Geranium thunbergii, 500.0 mg/dose Geraniin and furosin from Phyllanthus muellerianus, and 500.0 mg/dose gallic ellagic from Rasberry extract; inoculating the agar spread plate with the probiotic organism harvested from the growth broth; growing the probiotic organism on the agar spread plate; harvesting the probiotic organism from the agar spread plate; and freeze-drying the probiotic organism.
 14. The method of claim 13, further comprising: using the probiotic organism in a nutritional supplement product.
 15. The method of claim 13, further comprising: using the probiotic organism in a topical application product. 